ClinVar for Gene (Select 23258) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3359444	NM_015213.4(DENND5A):c.1994A>G (p.Tyr665Cys)	DENND5A (Y569C +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3359443	NM_015213.4(DENND5A):c.1607T>C (p.Ile536Thr)	DENND5A (I440T +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3337020	NM_015213.4(DENND5A):c.949+1G>T	DENND5A	Single nucleotide variant (splice donor variant)	not provided	GLikely pathogenic
Select item 3271606	NM_015213.4(DENND5A):c.1774C>T (p.His592Tyr)	DENND5A (H592Y +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3271605	NM_015213.4(DENND5A):c.3080A>G (p.Glu1027Gly)	DENND5A (E1003G +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3271604	NM_015213.4(DENND5A):c.3088A>G (p.Met1030Val)	DENND5A (M934V +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3271603	NM_015213.4(DENND5A):c.2564C>T (p.Ser855Leu)	DENND5A (S855L +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3271602	NM_015213.4(DENND5A):c.3336C>G (p.Ile1112Met)	DENND5A (I1088M +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3271601	NM_015213.4(DENND5A):c.3827C>T (p.Thr1276Met)	DENND5A (T1180M +2 more)	Single nucleotide variant (3 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 3271599	NM_015213.4(DENND5A):c.3599G>A (p.Arg1200Gln)	DENND5A (R1176Q +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3242315	GRCh37/hg19 11p15.4(chr11:8548056-10497905)x3	ADM, AKIP1 +18 more	Copy number gain	not provided	GUncertain significance
Select item 3081667	NM_015213.4(DENND5A):c.815A>G (p.Gln272Arg)	DENND5A (Q176R +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3081666	NM_015213.4(DENND5A):c.629T>C (p.Ile210Thr)	DENND5A (I186T +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3081665	NM_015213.4(DENND5A):c.2088G>T (p.Trp696Cys)	DENND5A, LOC126861134 (W600C +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3081664	NM_015213.4(DENND5A):c.192T>G (p.Phe64Leu)	DENND5A (F64L +1 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 3081663	NM_015213.4(DENND5A):c.1693C>T (p.Pro565Ser)	DENND5A (P469S +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3081662	NM_015213.4(DENND5A):c.1387C>G (p.Leu463Val)	DENND5A (L367V +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3081661	NM_015213.4(DENND5A):c.1259T>C (p.Ile420Thr)	DENND5A (I324T +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3064970	NM_015213.4(DENND5A):c.3387+3G>T	DENND5A	Single nucleotide variant (intron variant)	Developmental and epileptic encephalopathy, 49	GUncertain significance
Select item 3061326	NM_015213.4(DENND5A):c.2614C>T (p.Gln872Ter)	DENND5A (Q776* +2 more)	Single nucleotide variant (nonsense +1 more)	DENND5A-related disorder	GLikely pathogenic
Select item 3039777	NM_015213.4(DENND5A):c.*2C>A	DENND5A	Single nucleotide variant (3 prime UTR variant +1 more)	DENND5A-related disorder	GLikely benign
Select item 3026686	NM_015213.4(DENND5A):c.3060G>A (p.Leu1020=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3026034	NM_015213.4(DENND5A):c.995T>C (p.Met332Thr)	DENND5A (M236T +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3023960	NM_015213.4(DENND5A):c.465C>T (p.His155=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3010508	NM_015213.4(DENND5A):c.2862C>A (p.Ile954=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3010454	NM_015213.4(DENND5A):c.2152-4A>G	DENND5A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3007328	NM_015213.4(DENND5A):c.109+16G>C	DENND5A, LOC130005268	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3005872	NM_015213.4(DENND5A):c.2735+20A>G	DENND5A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3005354	NM_015213.4(DENND5A):c.3681-13C>T	DENND5A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3000265	NM_015213.4(DENND5A):c.2082C>T (p.Ala694=)	LOC126861134, DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2999564	NM_015213.4(DENND5A):c.2568C>T (p.Leu856=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2998265	NM_015213.4(DENND5A):c.2736-20T>C	DENND5A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2993029	NM_015213.4(DENND5A):c.2478C>T (p.Asp826=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2992166	NM_015213.4(DENND5A):c.2106G>A (p.Gln702=)	DENND5A, LOC126861134	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2991449	NM_015213.4(DENND5A):c.2556T>C (p.Asp852=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2988241	NM_015213.4(DENND5A):c.216A>G (p.Thr72=)	DENND5A	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2986114	NM_015213.4(DENND5A):c.1102C>T (p.Leu368=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2982741	NM_015213.4(DENND5A):c.949+16C>T	DENND5A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2981662	NM_015213.4(DENND5A):c.1287T>C (p.Ser429=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2979615	NM_015213.4(DENND5A):c.492A>G (p.Leu164=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2977566	NM_015213.4(DENND5A):c.2484G>A (p.Arg828=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2977528	NM_015213.4(DENND5A):c.546C>T (p.Asp182=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2975079	NM_015213.4(DENND5A):c.675A>G (p.Gln225=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2974520	NM_015213.4(DENND5A):c.3708C>T (p.Ala1236=)	DENND5A (P1225L)	Single nucleotide variant (missense variant +2 more)	not provided	GLikely benign
Select item 2974455	NM_015213.4(DENND5A):c.2070G>A (p.Arg690=)	DENND5A, LOC126861134	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2974395	NM_015213.4(DENND5A):c.21A>T (p.Gly7=)	DENND5A, LOC130005268	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2972504	NM_015213.4(DENND5A):c.2838C>G (p.Thr946=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2971285	NM_015213.4(DENND5A):c.3627C>T (p.Pro1209=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2971145	NM_015213.4(DENND5A):c.2436+9T>G	DENND5A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2970633	NM_015213.4(DENND5A):c.181+17A>G	DENND5A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2970494	NM_015213.4(DENND5A):c.2259C>T (p.Gly753=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2970386	NM_015213.4(DENND5A):c.2001G>A (p.Pro667=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2969751	NM_015213.4(DENND5A):c.1456-13T>A	DENND5A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2969548	NM_015213.4(DENND5A):c.181+14A>T	DENND5A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2968303	NM_015213.4(DENND5A):c.3129G>A (p.Pro1043=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2968135	NM_015213.4(DENND5A):c.1281T>C (p.His427=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2967892	NM_015213.4(DENND5A):c.627C>T (p.Leu209=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2964073	NM_015213.4(DENND5A):c.363T>C (p.Ile121=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2963535	NM_015213.4(DENND5A):c.2521+8A>G	DENND5A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2962697	NM_015213.4(DENND5A):c.652G>T (p.Ala218Ser)	DENND5A (A122S +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2959917	NM_015213.4(DENND5A):c.537T>C (p.Asp179=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2957229	NM_015213.4(DENND5A):c.1672-4C>T	DENND5A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2954808	NM_015213.4(DENND5A):c.1819C>G (p.Arg607Gly)	DENND5A (R583G +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2917709	NM_015213.4(DENND5A):c.3681-10G>A	DENND5A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2901633	NM_015213.4(DENND5A):c.3420G>A (p.Glu1140=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2900049	NM_015213.4(DENND5A):c.1587A>G (p.Ala529=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2899150	NM_015213.4(DENND5A):c.1803C>T (p.Leu601=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2894462	NM_015213.4(DENND5A):c.2736-9C>G	DENND5A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2891407	NM_015213.4(DENND5A):c.612T>G (p.Ser204=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2878657	NM_015213.4(DENND5A):c.2397C>T (p.Leu799=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2877835	NM_015213.4(DENND5A):c.2439G>A (p.Gly813=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2875783	NM_015213.4(DENND5A):c.109+18C>T	DENND5A, LOC130005268	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2863171	NM_015213.4(DENND5A):c.127C>T (p.Gln43Ter)	DENND5A (Q43*)	Single nucleotide variant (nonsense +3 more)	not provided	GPathogenic
Select item 2860857	NM_015213.4(DENND5A):c.2913C>T (p.Phe971=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2857477	NM_015213.4(DENND5A):c.3388-6A>G	DENND5A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2847156	NM_015213.4(DENND5A):c.1180T>C (p.Leu394=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2843644	NM_015213.4(DENND5A):c.2152-6A>G	DENND5A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2842993	NM_015213.4(DENND5A):c.961C>T (p.Leu321=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2840262	NM_015213.4(DENND5A):c.951T>C (p.His317=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2837980	NM_015213.4(DENND5A):c.1455+20C>T	DENND5A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2835040	NM_015213.4(DENND5A):c.1138-22_1138-20del	DENND5A	Microsatellite (intron variant)	not provided	GLikely benign
Select item 2825944	NM_015213.4(DENND5A):c.1167C>T (p.Asn389=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2822055	NM_015213.4(DENND5A):c.3511+16G>A	DENND5A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2820834	NM_015213.4(DENND5A):c.1308G>A (p.Lys436=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2817027	NM_015213.4(DENND5A):c.3237C>A (p.Thr1079=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2817022	NM_015213.4(DENND5A):c.624C>T (p.Cys208=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2816602	NM_015213.4(DENND5A):c.1158C>T (p.Asp386=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2815429	NM_015213.4(DENND5A):c.2409C>T (p.Ile803=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2814732	NM_015213.4(DENND5A):c.3681-3C>G	DENND5A	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2814262	NM_015213.4(DENND5A):c.1215G>A (p.Leu405=)	DENND5A	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2813476	NM_015213.4(DENND5A):c.182-16A>G	DENND5A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2812884	NM_015213.4(DENND5A):c.2606+11dup	DENND5A	Duplication (intron variant)	not provided	GLikely benign
Select item 2811390	NM_015213.4(DENND5A):c.3735A>T (p.Ala1245=)	DENND5A (H1234L)	Single nucleotide variant (missense variant +2 more)	not provided	GLikely benign
Select item 2807494	NM_015213.4(DENND5A):c.2259C>A (p.Gly753=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2807377	NM_015213.4(DENND5A):c.3123-19T>A	DENND5A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2802206	NM_015213.4(DENND5A):c.1906+18A>G	DENND5A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2801108	NM_015213.4(DENND5A):c.2751C>G (p.Arg917=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2800165	NM_015213.4(DENND5A):c.109+18C>G	DENND5A, LOC130005268	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2796980	NM_015213.4(DENND5A):c.1857T>C (p.Pro619=)	DENND5A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2796252	NM_015213.4(DENND5A):c.141C>T (p.Ala47=)	DENND5A	Single nucleotide variant (synonymous variant +3 more)	not provided	GUncertain significance

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